染色质
计算生物学
基因座(遗传学)
基因组
清脆的
锌指
基因组学
生物
染色体构象捕获
遗传学
基因
转录因子
增强子
作者
Vladimir S. Viushkov,Nikolai A. Lomov,Mikhail A. Rubtsov,Yegor Vassetzky
出处
期刊:Cells
[MDPI AG]
日期:2022-12-16
卷期号:11 (24): 4086-4086
被引量:8
标识
DOI:10.3390/cells11244086
摘要
Over the years, our vision of the genome has changed from a linear molecule to that of a complex 3D structure that follows specific patterns and possesses a hierarchical organization. Currently, genomics is becoming “four-dimensional”: our attention is increasingly focused on the study of chromatin dynamics over time, in the fourth dimension. Recent methods for visualizing the movements of chromatin loci in living cells by targeting fluorescent proteins can be divided into two groups. The first group requires the insertion of a special sequence into the locus of interest, to which proteins that recognize the sequence are recruited (e.g., FROS and ParB-INT methods). In the methods of the second approach, “programmed” proteins are targeted to the locus of interest (i.e., systems based on CRISPR/Cas, TALE, and zinc finger proteins). In the present review, we discuss these approaches, examine their strengths and weaknesses, and identify the key scientific problems that can be studied using these methods.
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